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S And M Enterprise

⚠️ Moderate Risk

FEI: 3003922230 • Freetown • SIERRA LEONE

FEI

FEI Number

3003922230

📍

Location

Freetown

🇸🇱
🏢

Address

10c Government Wharf, , Freetown, , Sierra Leone

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
2
Unique Violations
4/15/2004
Latest Refusal
1/22/2004
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

2971×

AFLATOXIN

The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.

3061×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
4/15/2004
16AFP67CATFISH, SALT WATER
306INSANITARY
Baltimore District Office (BLT-DO)
1/22/2004
23CHT07PEANUT, BUTTER
297AFLATOXIN
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is S And M Enterprise's FDA import refusal history?

S And M Enterprise (FEI: 3003922230) has 2 FDA import refusal record(s) in our database, spanning from 1/22/2004 to 4/15/2004.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. S And M Enterprise's FEI number is 3003922230.

What types of violations has S And M Enterprise received?

S And M Enterprise has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about S And M Enterprise come from?

All FDA import refusal data for S And M Enterprise is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.